Evidence map›Paper›PMID 38378479›Full record

ArticleBMC bioinformatics2024

Fusing graph transformer with multi-aggregate GCN for enhanced drug-disease associations prediction.

Shihui He, Lijun Yun, Haicheng Yi

Abstract read
In one paragraph

Article in BMC bioinformatics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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3 · Its place in the literature

Who cites it

8 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors.

Shihui HeSchool of Information Science and Technology, Yunnan Normal University, Kunming, 650500, China.
Lijun YunSchool of Information Science and Technology, Yunnan Normal University, Kunming, 650500, China. yunlijun@ynnu.edu.cn.
Haicheng YiSchool of Computer Science, Northwestern Polytechnical University, Xi'an, 710129, China. haichengyi@gmail.com.

Funding

Fundamental Research Funds for the Central Universities D5000230193Natural Science Basic Research Program of Shaanxi 2024JC-YBQN-0614
6 · The paper itself

Abstract

backgroundIdentification of potential drug-disease associations is important for both the discovery of new indications for drugs and for the reduction of unknown adverse drug reactions. Exploring the potential links between drugs and diseases is crucial for advancing biomedical research and improving healthcare. While advanced computational techniques play a vital role in revealing the connections between drugs and diseases, current research still faces challenges in the process of mining potential relationships between drugs and diseases using heterogeneous network data.

resultsIn this study, we propose a learning framework for fusing Graph Transformer Networks and multi-aggregate graph convolutional network to learn efficient heterogenous information graph representations for drug-disease association prediction, termed WMAGT. This method extensively harnesses the capabilities of a robust graph transformer, effectively modeling the local and global interactions of nodes by integrating a graph convolutional network and a graph transformer with self-attention mechanisms in its encoder. We first integrate drug-drug, drug-disease, and disease-disease networks to construct heterogeneous information graph. Multi-aggregate graph convolutional network and graph transformer are then used in conjunction with neural collaborative filtering module to integrate information from different domains into highly effective feature representation.

conclusionsRigorous cross-validation, ablation studies examined the robustness and effectiveness of the proposed method. Experimental results demonstrate that WMAGT outperforms other state-of-the-art methods in accurate drug-disease association prediction, which is beneficial for drug repositioning and drug safety research.

Indexed as

Biomedical ResearchDrug-Related Side Effects and Adverse ReactionsDrug RepositioningElectric Power SuppliesHumansLearningDrug–disease associationsDrug repositioningGraph neural networksGraph transformerNeural collaborative filtering

Identifiers

PMID38378479
PMCPMC10877759

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.